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FDA 510(k)

ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES

K-Number: K060094 · 2006-05-08

ApplicantArcadia Medical Corporation
Decision Date2006-05-08
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Arcadia Medical Corporation. It received FDA 510(k) clearance on 2006-05-08 under 510(k) number K060094. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES?

ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES is a medical device that received FDA 510(k) clearance on 2006-05-08. The listed applicant is Arcadia Medical Corporation. The 510(k) number is K060094.

When did ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES receive FDA 510(k) clearance?

ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES received FDA 510(k) clearance on 2006-05-08, under 510(k) number K060094.

Who is the listed applicant for ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES?

The FDA 510(k) record lists Arcadia Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES?

The FDA product code for ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES is BTR.

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Other records listing Arcadia Medical Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K031553SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES

Related Devices (Code: BTR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251794Tenax® Laser Resistant Endotracheal TubeBryan Medical, Inc.K253437Spiro-VISTASpiro RoboticsK250173Shiley™ Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley™ Nasal RAE Tracheal Tube Cuffless, Murphy Eye (114-XX) Shiley™ Oral RAE Tracheal Tube Cuffed, Murphy Eye (115-XX) Shiley™ Oral RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (115-XXOR) Shiley™ Nasal RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (119-XXNR)Covidien, LLCK243785Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™ Tracheal Tube TaperGuard™ Cuff Reinforced with Stylet Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley™ Oral/Nasal Tracheal Tube Cuffless ReinforcedCovidien, LLCK243579AeroJet Ventilation CatheterPipeline Medical Products, LLCK251499Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer (C-CAE-14.0-70-FI); Frova Intubating Introducer (C-CAE-14.0-70-FIC); Frova Intubating Introducer (C-CAE-14.0-70-FIC-SPOPS)William Cook Europe Aps

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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